Variant report

Variant	esv3525242
Chromosome Location	chr15:40762460-40764458
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:448)
CpG islands
(count:796)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:40762809-40762959	K562	blood:	n/a	n/a
2	BACH1	chr15:40762822-40763044	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr15:40762984-40763346	GM12878	blood:	n/a	chr15:40763244-40763257 chr15:40763176-40763189 chr15:40763166-40763179
4	BHLHE40	chr15:40763769-40763773	K562	blood:	n/a	n/a
5	BHLHE40	chr15:40763583-40763783	GM12878	blood:	n/a	n/a
6	CBX3	chr15:40763666-40764061	K562	blood:	n/a	n/a
7	CCNT2	chr15:40762681-40763928	K562	blood:	n/a	chr15:40763395-40763404
8	CEBPB	chr15:40762493-40762862	HepG2	liver:	n/a	chr15:40762676-40762687
9	CEBPB	chr15:40762528-40762820	ECC-1	luminal epithelium:	n/a	chr15:40762676-40762687
10	CEBPB	chr15:40762504-40762871	K562	blood:	n/a	chr15:40762676-40762687
11	CEBPB	chr15:40762501-40762862	IMR90	lung:	n/a	chr15:40762676-40762687
12	CEBPB	chr15:40762614-40762780	HepG2	liver:	n/a	chr15:40762676-40762687
13	CEBPB	chr15:40762503-40762881	HepG2	liver:	n/a	chr15:40762676-40762687
14	CEBPB	chr15:40762503-40762871	Hela-S3	cervix:	n/a	chr15:40762676-40762687
15	CEBPB	chr15:40762543-40762812	K562	blood:	n/a	chr15:40762676-40762687
16	CEBPB	chr15:40762567-40762816	A549	lung:	n/a	chr15:40762676-40762687
17	CEBPB	chr15:40762456-40762900	K562	blood:	n/a	chr15:40762676-40762687
18	CEBPD	chr15:40762892-40763277	HepG2	liver:	n/a	n/a
19	CHD1	chr15:40763682-40764031	GM12878	blood:	n/a	n/a
20	CHD2	chr15:40762612-40762802	K562	blood:	n/a	n/a
21	CHD2	chr15:40763686-40763726	GM12878	blood:	n/a	n/a
22	CHD2	chr15:40762605-40762776	GM12878	blood:	n/a	n/a
23	CHD2	chr15:40763670-40763678	K562	blood:	n/a	n/a
24	CHD2	chr15:40763993-40764242	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr15:40762901-40763172	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr15:40762793-40762815	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr15:40763556-40763566	HepG2	liver:	n/a	n/a
28	CHD2	chr15:40762894-40763073	HepG2	liver:	n/a	n/a
29	CREB1	chr15:40762950-40763308	A549	lung:	n/a	n/a
30	CTCF	chr15:40762966-40763114	GM12891	blood:	n/a	chr15:40763050-40763063
31	CTCF	chr15:40762944-40763170	HepG2	liver:	n/a	chr15:40763050-40763063
32	CTCF	chr15:40763000-40763150	GM12872	blood:	n/a	chr15:40763050-40763063
33	CTCF	chr15:40763798-40763865	GM12892	blood:	n/a	n/a
34	CTCF	chr15:40763940-40764090	SAEC	small airway:	n/a	n/a
35	CTCF	chr15:40763004-40763101	K562	blood:	n/a	chr15:40763050-40763063
36	CTCF	chr15:40764324-40764369	NHEK	skin:	n/a	n/a
37	CTCF	chr15:40764304-40764425	MCF-7	breast:	n/a	n/a
38	CTCF	chr15:40762982-40763069	GM12878	blood:	n/a	chr15:40763050-40763063
39	CTCF	chr15:40763238-40763263	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr15:40763760-40763910	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr15:40762856-40763266	K562	blood:	n/a	chr15:40763050-40763063
42	CTCF	chr15:40763775-40763908	GM19239	blood:	n/a	n/a
43	CTCF	chr15:40762920-40763070	GM12872	blood:	n/a	chr15:40763050-40763063
44	CTCF	chr15:40762989-40763054	HepG2	liver:	n/a	n/a
45	CTCF	chr15:40763847-40763974	GM12891	blood:	n/a	n/a
46	CTCF	chr15:40763007-40763062	GM13977	blood:	n/a	n/a
47	CTCF	chr15:40763788-40763831	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr15:40762940-40763090	HepG2	liver:	n/a	chr15:40763050-40763063
49	CTCF	chr15:40763035-40763056	MCF-7	breast:	n/a	n/a
50	CTCF	chr15:40763909-40763922	GM19239	blood:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:40763244-40763294	HIPEpiC	eye:	n/a
2	chr15:40762807-40762857	AoSMC	blood vessel:	n/a
3	chr15:40764195-40764245	AG10803	skin:	n/a
4	chr15:40763244-40763294	HIPEpiC	eye:	n/a
5	chr15:40762807-40762857	AoSMC	blood vessel:	n/a
6	chr15:40764195-40764245	AG10803	skin:	n/a
7	chr15:40762864-40762914	LNCaP	prostate:	n/a
8	chr15:40762864-40762914	BJ	skin:	n/a
9	chr15:40763763-40763813	MCF10A-Er-Src	breast:	n/a
10	chr15:40763244-40763294	AG09319	gingival:	n/a
11	chr15:40762807-40762857	NHBE	bronchial:	n/a
12	chr15:40763388-40763438	HUVEC	blood vessel:	n/a
13	chr15:40762864-40762914	HEEpiC	esophagus:	n/a
14	chr15:40763247-40763297	NH-A	brain:	n/a
15	chr15:40763388-40763438	HIPEpiC	eye:	n/a
16	chr15:40763995-40764045	MCF10A-Er-Src	breast:	n/a
17	chr15:40763073-40763123	HAEpiC	amniotic membrane:	n/a
18	chr15:40762864-40762914	NHBE	bronchial:	n/a
19	chr15:40763522-40763572	Jurkat	blood:	n/a
20	chr15:40763995-40764045	HCM	heart:	n/a
21	chr15:40763247-40763297	SK-N-MC	brain:	n/a
22	chr15:40763522-40763572	ovcar-3	ovarian:	n/a
23	chr15:40763199-40763249	PANC-1	pancreas:	n/a
24	chr15:40763763-40763813	T-47D	breast:	n/a
25	chr15:40762807-40762857	SK-N-SH	brain:	n/a
26	chr15:40763388-40763438	U87	brain:	n/a
27	chr15:40763073-40763123	IMR90	lung:	fetal
28	chr15:40763763-40763813	HRPEpiC	eye:	n/a
29	chr15:40763763-40763813	AG09319	gingival:	n/a
30	chr15:40763051-40763101	AG09319	gingival:	n/a
31	chr15:40763073-40763123	Jurkat	blood:	n/a
32	chr15:40764195-40764245	AG04450	lung:	fetal
33	chr15:40764195-40764245	GM12892	blood:	n/a
34	chr15:40762807-40762857	PANC-1	pancreas:	n/a
35	chr15:40763522-40763572	NB4	blood:	n/a
36	chr15:40763995-40764045	A549	lung:	n/a
37	chr15:40763244-40763294	K562	blood:	n/a
38	chr15:40763051-40763101	HCPEpiC	choroid plexus:	n/a
39	chr15:40763522-40763572	T-47D	breast:	n/a
40	chr15:40763995-40764045	NH-A	brain:	n/a
41	chr15:40763199-40763249	HEEpiC	esophagus:	n/a
42	chr15:40763995-40764045	PFSK-1	brain:	n/a
43	chr15:40763247-40763297	AoSMC	blood vessel:	n/a
44	chr15:40763522-40763572	SK-N-SH_RA	brain:	n/a
45	chr15:40764195-40764245	AoSMC	blood vessel:	n/a
46	chr15:40763244-40763294	NHBE	bronchial:	n/a
47	chr15:40763388-40763438	RPTEC	kidney:	n/a
48	chr15:40763388-40763438	SK-N-MC	brain:	n/a
49	chr15:40763522-40763572	SAEC	small airway:	n/a
50	chr15:40763244-40763294	HPAEpiC	pulmonary alveolar:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:40746042..40747567-chr15:40761663..40764195,2	MCF-7	breast:
2	chr15:40763768..40766540-chr15:40784281..40786409,2	K562	blood:
3	chr15:40763158..40763829-chr15:66796805..66797653,2	HCT-116	colon:
4	chr15:40731794..40734704-chr15:40761511..40763222,2	MCF-7	breast:
5	chr15:40731823..40734826-chr15:40760868..40766207,7	K562	blood:
6	chr15:40761396..40764374-chr15:40800140..40802676,2	K562	blood:
7	chr15:40761789..40767637-chr15:40797359..40801640,7	K562	blood:
8	chr15:40763466..40765784-chr15:40773295..40775990,2	MCF-7	breast:
9	chr15:40731621..40739951-chr15:40753297..40765462,23	K562	blood:
10	chr15:40762952..40763883-chr6:26056601..26057141,2	NB4	blood:
11	chr15:40757114..40759999-chr15:40761935..40763724,3	MCF-7	breast:
12	chr15:40721609..40723938-chr15:40763922..40765689,2	K562	blood:
13	chr15:40721609..40724539-chr15:40764189..40766844,2	K562	blood:
14	chr15:40749483..40752811-chr15:40761476..40764713,3	MCF-7	breast:
15	chr15:40763301..40766173-chr15:40861522..40864181,2	K562	blood:

No data

Variant related genes	Relation type
CHST14	TF binding region
ENSG00000259211	TF binding region
CHST14	CpG island
ENSG00000259211	CpG island
ENSG00000174444	chromatin interactions
ENSG00000140320	chromatin interactions
ENSG00000174442	chromatin interactions
ENSG00000166133	chromatin interactions
ENSG00000244251	chromatin interactions
ENSG00000259536	chromatin interactions
ENSG00000187837	chromatin interactions
ENSG00000259364	chromatin interactions
ENSG00000259211	chromatin interactions

Extended variants
information (count: 84 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:84 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572337338	chr15:40762463-40762464	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs542201344	chr15:40762511-40762512	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs541191259	chr15:40762546-40762547	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs559839247	chr15:40762549-40762550	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs532034594	chr15:40762581-40762582	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs545795854	chr15:40762598-40762599	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs9672313	chr15:40762621-40762622	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs531334558	chr15:40762681-40762682	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs59322420	chr15:40762705-40762706	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs397963102	chr15:40762707-40762708	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs369568423	chr15:40762732-40762733	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs373120964	chr15:40762768-40762769	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs143661163	chr15:40762838-40762839	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs633295	chr15:40762842-40762843	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs547566991	chr15:40762854-40762855	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs56908156	chr15:40762862-40762863	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs539588795	chr15:40762870-40762871	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs118118557	chr15:40762879-40762880	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs565101523	chr15:40762913-40762914	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs569976002	chr15:40762974-40762975	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs185409383	chr15:40763001-40763002	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs555798890	chr15:40763228-40763229	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs12902521	chr15:40763238-40763239	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs572374791	chr15:40763329-40763330	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs541231571	chr15:40763380-40763381	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs557892405	chr15:40763381-40763382	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs577809616	chr15:40763470-40763471	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs545629118	chr15:40763511-40763512	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs562582335	chr15:40763516-40763517	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs397518432	chr15:40763557-40763558	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs199749498	chr15:40763563-40763564	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs139908298	chr15:40763575-40763576	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs267606730	chr15:40763617-40763618	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs191997027	chr15:40763622-40763623	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs371189136	chr15:40763651-40763652	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs561964206	chr15:40763662-40763663	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs371684007	chr15:40763700-40763701	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs201632751	chr15:40763737-40763738	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs112549048	chr15:40763743-40763744	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs35318007	chr15:40763747-40763748	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs112899398	chr15:40763778-40763779	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs564319358	chr15:40763782-40763783	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs368203130	chr15:40763812-40763813	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs267606727	chr15:40763815-40763816	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs267606728	chr15:40763822-40763823	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs533124457	chr15:40763838-40763839	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs550038340	chr15:40763839-40763840	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs146457413	chr15:40763849-40763850	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs200761477	chr15:40763883-40763884	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs183422103	chr15:40763904-40763905	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD

Chromatin state (count:518 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40747400-40762600	Weak transcription	HUVEC	blood vessel
2	chr15:40749200-40762600	Weak transcription	Psoas Muscle	Psoas
3	chr15:40749200-40762800	Weak transcription	Small Intestine	intestine
4	chr15:40758600-40762600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr15:40759000-40762600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr15:40759200-40762600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr15:40759400-40762600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr15:40759400-40763400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr15:40759600-40762600	Weak transcription	Primary B cells from peripheral blood	blood
10	chr15:40759600-40762600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr15:40759600-40762600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr15:40759600-40762600	Weak transcription	Ovary	ovary
13	chr15:40759600-40762600	Weak transcription	GM12878-XiMat	blood
14	chr15:40759800-40762600	Weak transcription	Fetal Thymus	thymus
15	chr15:40759800-40762600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr15:40760000-40762600	Weak transcription	HSMMtube	muscle
17	chr15:40760200-40762600	Weak transcription	Thymus	Thymus
18	chr15:40760600-40762600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr15:40760800-40762600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr15:40760800-40762600	Enhancers	K562	blood
21	chr15:40761000-40762600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr15:40761200-40762800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr15:40761200-40762800	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr15:40761200-40762800	Enhancers	NHEK	skin
25	chr15:40761400-40762800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:40761600-40762600	Weak transcription	HMEC	breast
27	chr15:40761600-40763800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr15:40761800-40762600	Enhancers	Primary hematopoietic stem cells	blood
29	chr15:40761800-40762800	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr15:40761800-40763000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr15:40762000-40762600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr15:40762000-40762600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr15:40762000-40762600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr15:40762000-40762800	Enhancers	HSMM	muscle
35	chr15:40762000-40763000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr15:40762200-40762600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr15:40762200-40762600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr15:40762200-40762600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr15:40762200-40762600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr15:40762200-40762600	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr15:40762200-40762600	Enhancers	Muscle Satellite Cultured Cells	--
42	chr15:40762200-40762600	Enhancers	Colon Smooth Muscle	Colon
43	chr15:40762200-40762600	Enhancers	Fetal Brain Male	brain
44	chr15:40762200-40762600	Enhancers	Placenta	Placenta
45	chr15:40762200-40762600	Enhancers	Fetal Stomach	stomach
46	chr15:40762200-40762600	Enhancers	Placenta Amnion	Placenta Amnion
47	chr15:40762200-40762600	Enhancers	Stomach Mucosa	stomach
48	chr15:40762200-40762600	Enhancers	Dnd41	blood
49	chr15:40762200-40762600	Enhancers	NH-A	brain
50	chr15:40762200-40762800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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